Increase In Emission Intensity Research Articles

Water-Soluble Chitosan-Europium Hybrid Sensor for Singlet Oxygen Detection.

The ability to effectively monitor singlet oxygen (1O2) with fluorescence probes in biological systems is severely restricted mainly by the background autofluorescence of these systems. Though the application of lanthanide complexes as 1O2 monitors successfully resolves this problem with time-gated luminescence measurements, the insolubility of these complexes in an aqueous medium heavily limits their application in biological systems. Here, we present a water-soluble 1O2 sensor based on a chitosan-europium hybrid material. A procedure for the modification of chitosan to expand its solubility to neutral and basic pH, while maintaining its free active amine groups, is described. These are then coupled covalently to a europium-based probe for the detection of 1O2. The resulting hybrid sensor is readily soluble in water across the pH scale and efficiently signals the presence of 1O2 at physiological pH, with the characteristic Eu3+ emission at 611 nm yielding up to a 15-fold increase in emission intensity and a decay time of 332 μs. Being of particular interest for time-gated measurements, this long decay time, coupled with the biocompatibility of chitosan, describes a material with potential biological applications, where 1O2 plays a vital role.

Optical, electrical, structural properties by of PFO-PMMA films loaded with TiO2 nanoparticles

The authors studied Poly (methyl methacrylate) also called PMMA films with different concentrations of Poly (9, 9′-di-n-octylfuorenyl-2, 7-diyl) also called PFO and concluded that 1% PFO blended with PMMA is the best choice for opto-electronic applications. In the present study, the authors prepared nanocomposite films of PMMA + 1% PFO + different concentrations of TiO2 nanoparticles. The resulting films were subjected to FTIR, XRD, UV–visible, fluorescence and electrical conductivity studies. The polymer matrix undergoes modifications in its molecular and microstructural characteristics as evidenced by FTIR and XRD results. The addition of TiO2 nanoparticles leads to a uniform dispersion and good interaction with the blend matrix resulting in homogeneous films. The additional peaks were found at a wavenumber of 3620 cm−1 in FTIR can be attributed to stretching vibration of TiO2. The presence of TiO2 nanoparticles is confirmed by the distinctive diffraction peaks observed at 25.4°, 37.8°, 48.3°, 54.3°, 55.2°, and 62.8°. With a shift in the absorption peak towards higher wavelengths, the nanocomposites show greater absorption in the UV and visible regions. As the concentration of TiO2 increases, the optical parameters such as absorption coefficient, extinction coefficient, Urbach energy, refractive index and optical conductivity also increase. The direct optical band gap of the PNC films decreases from 5.03 to 3.06 eV and indirect band gap decreases from 4.52 to 1.92 eV at 10 wt% of TiO2 concentration. The addition of TiO2 nanoparticles to the PFO/PMMA matrix resulted in an increase in fluorescence emission intensity. The AC electrical conductivity exhibits increasing trend with frequency in Audio-Frequency range. Thus TiO2 nanoparticles improve the overall optical, electrical, and structural properties of PFO-PMMA nanocomposites. This means that they can be used in a variety of optoelectronic and advanced optical devices.

Deciphering the point source carbon footprint puzzle: Land use dynamics and socio-economic drivers

Point source carbon emissions account for approximately 80 % of total emissions. Investigating the influence of land use and socio-economic indicators on these emissions is crucial for achieving sustainable development goals. Existing research faces challenges such as focusing on specific regions, mixing variables that may exhibit multicollinearity, and lacking sufficient land use information. This study takes China, the largest emitting country, as a case study, utilizing geospatial big data to subdivide land use into 11 categories based on emission sectors. The impacts of land use and socio-economic indicators on different emission sectors are discussed from the perspectives of bivariate and spatial statistical analysis, with spatial hotspots identified. Hierarchical regression is used to evaluate the explanatory power of the indicators and to establish models, and potential carbon reduction strategies are further explored. Key findings reveal: (1) Significant multicollinearity between land use and socio-economic indicators was demonstrated, with land use explaining 57.1 % of emissions compared to 37.4 % explained by socio-economic indicators. The spatial consistency between land use and emissions exceeds 80 %, and the spatiotemporal variability is relatively low, making land use a more advantageous factor in explaining point source carbon emissions. (2) Agricultural mechanization increases emission intensity, but this efficient farming method helps convert surplus plowland, the largest influencing factor (Coefficient = 0.717), into carbon sinks, thereby controlling agricultural emissions. (3) Land intensification helps control industrial land, the main factor influencing industrial emissions (Coefficient = 0.392). It also contributes to the efficient use of carbon reduction technologies and industrial supporting land. (4) Mixed commercial and residential land has the greatest impact on commercial, service, and household emissions. However, its relationship with the economy (Correlation = 0.479) is stronger than its relationship with emissions (Correlation = 0.182), making it more applicable to cities that serve as economic growth hubs.

Novel sulfonylurea fluorescence probes for antiproliferative activity, detection and imaging of fluoride ions in living cells

In this study, four novel triphenylpyrazoline 4-toluenesulfonylureas (PYSUs) were synthesized to develop potential anticancer drugs and fluorescent probes for the detection of F− ions. The compounds were synthesized via a two-step microwave-assisted method. The antiproliferative activity of the PYSUs was tested against two cancer cell lines: HepG2 and MDA-MB-231. Among the compounds, 3a exhibited strong activity against both cell lines, while 3b showed strong activity against MDA-MB-231 cells but weaker inhibition of HepG2 cells. Furthermore, compound 3b was identified as the best fluorescent probe, with an increase in emission intensity in the presence of F− ions from tetrabutylammonium fluoride (TBAF). In DMSO, the emission wavelength was found to be 518 nm (green) with an excitation wavelength of 469 nm. The limit of detection (LOD) was calculated to be 0.269 mM in the linear range of 5–10 mM. The interaction mechanism between F− ions and compound 3b was further explored via DFT/TDDFT calculations. Additionally, fluorescent imaging of TBAF-incubated MDA-MB-231 and HepG2 cells confirmed the potential of PYSUs as fluorescent sensors for F− ions in living cancer cells.

Features of Radio Emission Propagation in the Ionosphere under Conditions of Threshold Nonlinearity

The well-known problem of nonlinear “wave – ionosphere” interaction under conditions of threshold nonlinearity is considered. It is believed that nonlinear effects arise only for high-power radiation, when the wave amplitude exceeds a certain threshold value. The possibility of the existence of concentrated wave fields under these conditions is shown. It is revealed that a certain ratio of nonlinearity parameters leads to an increase in the radio emission intensity, since the interaction of individual solitons can lead to their merging into a higher-power solitary wave. The presence of threshold nonlinearity can lead to the formation of an ordered structure of solitary waves.

Bridging climate refuges for climate change adaptation: A spatio-temporal connectivity network approach

Enhancing the spatio-temporal connectivity of dynamic landscapes is crucial for species to adapt to climate change. However, a spatio-temporal connectivity network approach considering climate change and species movement is often overlooked. Taking Tibetan wild ass on the Qinghai-Xizang Plateau as an example, we simulated species distribution under current (2019) and future scenarios (2100), constructed spatio-temporal connectivity networks, and assessed the spatio-temporal connectivity. The results show that under the current, SSP2-4.5 and SSP3-7.0 scenarios, the suitable habitats for Tibetan wild ass account for 21.11%, 21.34%, and 20.95% of the total area, respectively, which show more fragmentation in 2100. 78.35% of habitats which are predicted to be suitable under current conditions will remain suitable in the future, which can be regarded as stable climate refuges. With the increase in future emission intensity, the number percentage of auxiliary connectivity corridors increases from 27.65% to 33.57%. This indicates that more patches will function as temporary refuges and the auxiliary connectivity corridors will gradually weaken the dominance of direct connectivity corridors. Under different SSP-RCP scenarios, the internal spatio-temporal connectivity is the highest, accounting for 42%–43%. Compared with the spatio-temporal perspective, the purely spatial perspective overestimates network connectivity by about 28% considering all current and future patches, and underestimates network connectivity by 16%–21% when only considering all current or future patches. In this study, a new approach of spatio-temporal connectivity network is proposed to bridge climate refuges, which contributes to the long-term effectiveness of conservation networks for species’ adaptation to climate change.

On the glow of cremated remains: long-lived green photo-luminescence of heat-treated human bones.

The long-lived green luminescence of human bone (that has been heated to 600°C for a short duration) is attributed to a carbon quantum dot material (derived from collagen) encapsulated and protected by an inorganic matrix (derived from bone apatite) and is more intense in dense rigid and crystalline parts of (healthy) human bones. The strong collagen-apatite interaction results (upon decomposition) in a protective inorganic environment of the luminescent centers allowing long-lived triplet-based emission of a carbon (quantum) dot-like material at room temperature, as well as resilience against oxidation between 550 and 650°C. The graphitic black phase (obtained upon heating around 400°C) is a precursor to the luminescent carbon-based material, that is strongly interacting with the crystalline inorganic matrix. Human bone samples that have been heated to 600°C were subjected to steady-state and time-resolved spectroscopy. Excitation-emission matrix (EEM) luminescence spectroscopy revealed a broad range of excitation and emission wavelengths, indicating a heterogeneous system with a broad density of emissive states. The effect of low temperature on the heat-treated bone was studied with Cryogenic Steady State Luminescence Spectroscopy. Cooling the bone to 80K leads to a slight increase in total emission intensity as well as an intensity increase towards to red part of the spectrum, incompatible with a defect state model displaying luminescent charge recombination in the inorganic matrix. Time-resolved spectroscopy with an Optical Multichannel Analyzer (OMA) and Time Correlated Single Photon Counting (TCSPC) of these samples showed that the decay could be fitted with a multi-exponential decay model as well as with second-order decay kinetics. Confocal Microscopy revealed distinct (plywood type) structures in the bone and high intensity-fast decay areas as well as a spatially heterogeneous distribution of green and (fewer) red emissive species. The use of the ATTO 565 dye aided in bone-structure visualization by chemical adsorption. Conceptually our data interpretation corresponds to previous reports from the material science field on luminescent powders.

Annealing Effect on Structural, Optical and Electrophysical Properties of ZnSe Nanocrystals Synthesized into SiO2/Si Ion Track Template.

We report the results of synthesis of zinc selenide (ZnSe) nanocrystals into SiO2/Si track templates formed by irradiation with 200 MeV Xe ions up to a fluence of 107 ions/cm2. Zinc selenide nanocrystals were obtained by chemical deposition from the alkaline aqueous solution. Scanning electron microscopy, X-ray diffractometry, Raman and photoluminescence spectroscopy, and electrical measurements were used for characterization of synthesized ZnSe/SiO2nanoporous/Si nanocomposites. XRD data for as-deposited precipitates revealed the formation of ZnSe nanocrystals with cubic crystal structure, spatial syngony F-43m (216). According to non-empirical calculations using GGA-PBE and HSE06 functionals, ZnSe crystal is a direct-zone crystal with a minimum bandgap width of 2.36 eV and anisotropic electronic distribution. It was found that a thermal treatment of synthesized nanocomposites at 800 °C results in an increase in ZnSe nanocrystallites size as well as an increase in emission intensity of created precipitates in a broad UV-VIS spectra range. However, vacuum conditions of annealing still do not completely prevent the oxidation of zinc selenide, and a formation of hexagonal ZnO phase is registered in the annealed samples. The current-voltage characteristics of the synthesized nanocomposites proved to have n-type conductivity, as well as increased conductivity after annealing.

Influence of Pr3+ co-doping on the luminescent properties of CGA:2 at.% Ho single crystal fibers

Ho3+, Pr3+ co-doped CaGdAlO4 (Ho,Pr:CGA) crystal fibers were successfully grown by the micro-pulling-down (μ-PD) technique for the first time. Detailed investigations were conducted on the polarized absorption spectra, fluorescence spectra, and lifetime decay curves. The 2 at.% Ho, 0.4 at.% Pr:CGA crystal fiber exhibits a broad absorption band at 1147 nm with full width at half maximum (FWHM) of 25.5 nm and 64.5 nm for σ and π polarization, respectively. Increasing the concentration of Pr3+ led to a decrease in emission intensity at 2001 nm and an increase in emission intensity at 2861 nm. The FWHMs of the crystal fiber containing 2 at.% Ho and 0.4 at.% Pr:CGA at 2861 nm were 44.5 nm for σ polarization and 24.3 nm for π polarization. Additionally, the lifetime ratio (5I7/5I6) decreases from 25.18 to 2.85 in the crystal fibers containing 2 at.% Ho:CGA and 2 at.% Ho, 0.4 at.% Pr:CGA, respectively. These findings suggest that the presence of deactivated Pr3+ ions can significantly reduce the lifetime gap between the 5I6 and 5I7 energy levels, potentially mitigating the self-termination phenomenon on the ∼3 μm emission.

Environmental regulation and intermediate imports: Firm-product-level evidence

This study examines the effects of domestic environmental regulations on import activity. Using a panel of firm-product-level data and variations in regulatory stringency across products established by China’s Eleventh Five-Year Plan for Environmental Protection (covering 2006–2010), it reveals that tougher regulations on emission-intensive industries at home led to increases in downstream manufacturers’ imports of emission-intensive intermediate inputs. Specifically, a 1% increase in sulfur dioxide emission intensity resulted in a 0.026% increase in intermediate imports after the implementation of the regulation. A back-of-the-envelope calculation suggests that, although the regulation increased emissions in source countries, it reduced global emissions of sulfur oxides and carbon dioxide. This is because the increases in imports caused by the regulation mainly came from countries with lower emission intensity than China. The regulation did not disproportionately increase imports from or emissions in developing countries.

Argon plasma-enhanced UV light emission from ZnO submicrowires grown by hydrothermal method

In this work, the optical, morphological, and structural improvements of vertically aligned, hydrothermally grown ZnO submicrowires (SMWs) treated with a 250 W, 250 V RF argon plasma (Ar) during different exposure times were investigated by scanning and transmission electrons microscopy, X-ray diffraction, and micro-Raman and photoluminescence (PL) spectroscopies. In two steps, the SMWs were synthesized in an aqueous medium at low temperatures. The plasma-treated samples showed significantly improved room-temperature PL compared to untreated samples. All the treated samples exhibited a substantial increase of the near band edge UV emission intensity and a decrease of the deep level emission in the visible. The samples treated for 4 minutes presented the best UV/vis intensity ratio of ∼ 1568 (an increase of ⁓174-fold with respect to the untreated sample). The analysis of the UV band in terms of the first and second phonon replica of the excitonic emission indicated that the Ar plasma treatment favors the multiple phonon-exciton coupling, with partial correlation with the observed overall increase of the UV/visible intensity ratio. From the PL measurements at low temperatures, the presence of excitons bound to H donors in the ZnO structure was inferred. The possible reasons for the Ar plasma-induced enhancement of the UV emission from the treated SMWs are discussed in terms of previous work, the observed morphology and changes expected to occur at the SMW surfaces due to Ar ion impacts from the plasma.

Analysis of the carbon emissions trend in the Indian manufacturing sector: a decomposition and decoupling approach.

There is a growing emphasis on fostering green growth and lowering carbon emissions in order to achieve sustainable economic development. This study uses the Tapio decoupling model and analyzes the factors influencing changes in carbon emissions from manufacturing in India utilizing the log mean Divisia index (LMDI) techniques. Furthermore, the nexus between carbon emission intensity, information and communication technology (ICT), total factor productivity (TFP), skill, and energy intensity has been analyzed using the system-GMM approach. It is based on the plant-level Annual Survey of Industries (ASI) datasets for the organized manufacturing sector of India from 2001 to 2002 to 2019 2020 for the major 21 Indian states/UT. The findings reflect the presence of weak decoupling in the manufacturing sector both at the aggregate level and in states. This indicates that both output and emissions are increasing; however, output growth surpasses emission growth, which signifies an effort to transition towards more environmentally friendly production methods and enhanced energy efficiency. The output and population effect are found to be leading factors in carbon emissions, while energy intensity is found to be reducing the effect. Further, the system-GMM estimates show that ICT and energy intensity positively affect total factor productivity, while with an increase in carbon emission intensity, productivity declines. The study confirms the existence of an inverted N-shaped Kuznets curve in the sector. This present study will contribute to formulating energy and environmental strategies to reduce emissions and promote adopting cleaner energy sources. These efforts will facilitate the attainment of carbon neutrality and enhance energy efficiency within the sector.

Effects of donor substituents on the conformational heterogeneity, photophysical, mechanochromic and electroluminescent properties of the donor-substituted fluorine-containing triphenylpyrimidines

Three derivatives of fluorinated triphenylpyrimidine with the attached carbazole, phenothiazine, or acridan donor moieties are synthesized by Buchwald-Hartwig reactions. The impact of the donor units on emissive and other properties of the compounds is reported. The compounds exhibit excellent thermal stability, competitive photophysical phenomena such as room temperature phosphorescence (RTP) appearing when compounds are molecularly dispersed in the rigid polymer matrix and thermally activated delayed fluorescence (TADF). The compounds with carbazole and phenothiazine donor moieties show the manifestation of triplet–triplet annihilation in the electroluminescence when used as emitters in organic light-emitting diodes (OLEDs). The phenothiazine-containing compound exhibit dual photoluminescence with the blue-shifted peak corresponding to the quasi-axial conformer and a red-shifted peak to the quasi-equatorial conformer. This derivative shows reversible shifts of emission spectra exceeding 100 nm due to the stable (at least 4 cycles) mechanochromic luminescence under the application of external stimuli. After grinding the emission intensity maximum is observed at 555 nm, after fuming at. ca 448 nm and after melting at 555 nm. The photoluminescence shifts and ON/OFF delayed fluorescence of the phenothiazine-based emitter occur due to the alteration between the crystalline and amorphous states. Optimization of the device structure allows to control the charge balance resulting in external quantum efficiency of up to 5.7 % observed for the OLED based on the phenothiazine-based emitter. This compound also shows the biggest response to the presence of oxygen acting as the quencher of triplet excited energy. The film of the compound doped in rigid Zeonex shows an 8.4-fold increase in emission intensity after evacuation. The optical sensor fabricated using the derivative of fluorinated triphenylpyrimidine and phenothiazine is characterized by the Stern-Volmer constant 1.37 × 10-4 ppm−1.

Qualitative Geochemical Analysis of the 2004 Indian Ocean Giant Tsunami Deposits Excavated at Seungko Mulat Located in Aceh Besar of Indonesia Using Laser-Induced Breakdown Spectroscopy

Laser-induced breakdown spectroscopy (LIBS) was employed to characterize the geochemical signatures layer by layer of 2004 Indian Ocean tsunami deposits in Seungko Mulat Village, Aceh Province, Indonesia. In the LIBS experimental setup, a Nd-YAG laser beam is directed towards the deposit samples, and the resulting atomic emission lines from the laser-induced plasma are captured using a spectrometer. Our analysis reveals terrestrial indicators (Fe), heavy metals (Cu, Cr, Co, Cd), and increased emission intensity of Mg, Ca, Al, K, Si, Ba, N, and O in the 2004 Indian Ocean tsunami layers. The emission intensity ratios of several elements in the 2004 Indian Ocean tsunami deposit layers, namely Ca/Ti, Si/Ti, and K/Ti, unveil notable disparities among the elements evaluated. This indicates the possibility of utilizing these ratios as reliable geochemical markers to differentiate the layer by layer of tsunami deposits. LIBS surpasses XRF in detecting nearly all elements simultaneously and identifying both light elements and specific heavy metals (Ba, Cu, Cr, Co, Cd, Pb, Ni, V, W), exceeding XRF's detection capabilities. This study emphasizes the effectiveness of LIBS as an advanced optical technique, offering speed and promise in analyzing layer-by-layer geochemical markers of the 2004 Indian Ocean tsunami deposits in Seungko Mulat Village.

Prediction of Suitable Habitat of Alien Invasive Plant Ambrosia trifida in Northeast China under Various Climatic Scenarios

Ambrosia trifida is an invasive alien plant species, which has very high reproductive and environmental adaptability. Through strong resource acquisition ability and allelopathy, it could inhibit the growth and reproduction of surrounding plants and destroy the stability of an invasive ecosystem. It is very important to predict the change of suitable distribution area of A. trifida with climate change before implementing scientific control measures. Based on 106 A. trifida distribution data and 14 points of environmental data, the optimal parameter combination (RM = 0.1, FC = LQ) was obtained using the MaxEnt (version 3.4.1) model optimized by Kuenm package, and thus the potential suitable areas of A. trifida in Northeast China under three different climate scenarios (RCP2.6, RCP4.5, RCP8.5) with different emission intensities in the future (2050, 2070) were predicted. The changes of A. trifida suitable area in Northeast China under three climate scenarios were compared, and the relationship between the change of suitable area and emission intensity was analyzed. In general, the suitable area of A. trifida in Northeast China will expand gradually in the future, and the area of its highly suitable area will also increase with the increasing emission intensity, which is unfavorable to the control of A. trifida.

Sb3+/Sm3+ Codoped Cs2NaScCl6 All-Inorganic Double Perovskite: Blue Emission of Self-Trapped Excitons and Red-Emission via Energy Transfer.

The lead-free halide perovskites possess nontoxicity and excellent chemical stability, whereas relatively weak luminescence intensity limits their potential in practical applications. Therefore, strengthening the luminescence intensity and expanding application fields are urgent tasks for the development of lead-free halide perovskites. In this paper, antimony-doped Cs2NaScCl6 crystals synthesized by a solvothermal method emit bright, deep blue photoluminescence at 447 nm. The photoluminescence (PL), photoluminescence excitation (PLE), and absorption spectra demonstrate that Sb3+ doping effectively activate the intrinsic "dark self-trapped exciton (STE)," leading to an impressive photoluminescence quantum yield (PLQY) value of 78.31% for 1% Sb3+ doping. Furthermore, the luminescence intensity remains above 92% compared with the fresh sample without secondary phases detected even after 90 days under environmental conditions. To expand the emission spectra, rare-earth Sm3+ is further incorporated into Cs2NaScCl6:1% Sb3+ crystals. The results show that Sb ions not only enhance intrinsic STE luminescence but also serve as sensitizers to boost the red-light emission of Sm3+, leading to a significant 500-fold increase in red emission intensity. Finally, the PLQY reaches a stunning 86.78%. These findings provide valuable insights in the design of Sb ion-doped lead-free double perovskites, broadening the application fields in various optoelectronic devices.

A series of triphenylamine-derived fluorophores attached to a Cu-based MOF for gaseous CO optical sensing: synthesis, performance, and mechanism.

A series of triphenylamine-derived fluorescent dyes were attached to a Cu2+-containing MOF (metal-organic framework), denoted as Pm@CuMOF. The molecular structures of these dyes were discussed by the single crystal structures. Their major absorption bands peaked at 410-450 nm, showing emission bands ranging from 556 to 586 nm with emission quantum yields ranging from 8.0 to 15.1%. It was found that the [-N(C2H5)2] group generally improved sensing performance, and the -OH group in the dyes helped the Cu2+ quenching effect. Pm@CuMOF was observed by SEM as nanorods with a width of ~100 nm and a length of 300 nm. Their XRD patterns and N2 adsorption/desorption isotherms were recorded to confirm their porous structure. A low probe loading level of ~4% was determined by TGA result. The CO sensing mechanism was revealed as a Cu2+/Cu+-involved sensing mechanism based on the result of NMR titration, IR, XPS, and EPR. The fluorescence of these triphenylamine-derived dyes was firstly quenched by CuMOF. In contact with CO, Cu2+ was reduced to Cu+, accompanied by the release and fluorescence recovery of the fluorescent dyes, showing emission turn-on effect towards CO gas. Pm@CuMOF showed increased emission intensity at CO level of 0.005% (versus N2), with response times ranging from 123 s to 280 s (depending on various temperatures). Good selectivity was observed over competing alkane gases, with stable emission for at least 5 days, but no linear calibration plots were observed.

Pollution Emission Intensity and Domestic Value-Added Rate of Firms' Exports: An Empirical Analysis Based on China’s Microdata

Abstract With the development of global economic integration, global value chains (GVC) have become the mainstay of the global economy. China's low-end embedded model relying on its labor advantage can no longer bring new economic benefits, and the ensuing environmental problems are intensifying. Therefore, there is an urgent need to explore a win-win path for the greening of China's economy and the improvement of GVC status. Using micro-firm data, the article explores the role of pollution emission intensity of China's firms in influencing the domestic value-added rate of their exports. The study finds that (1) the increase of pollution emission intensity of Chinese enterprises has a significant inhibiting effect on their export domestic value-added rate; (2) the pollution emission intensity of Chinese enterprises under different regions, different ownership and different trading methods has differentiated effects on their export domestic value-added rate. Among them, the pollution emission intensity of state-owned enterprises, enterprises in western regions and processing trade enterprises have a more significant inhibitory effect on the domestic value-added rate of their exports; (3) the increase of total factor productivity of enterprises can slow down the negative effect of enterprise pollution emission intensity on the domestic value-added rate of its export. Keywords: Enterprise Pollution Emission Intensity, Export Domestic Value-Added Rate, Global Value Chain Embeddedness.

Cost and competitiveness of green hydrogen and the effects of the European Union regulatory framework

By passing the delegated acts supplementing the revised Renewable Energy Directive, the European Commission has recently set a regulatory benchmark for the classification of green hydrogen in the European Union. Controversial reactions to the restricted power purchase for electrolyser operation reflect the need for more clarity about the effects of the delegated acts on the cost and the renewable characteristics of green hydrogen. To resolve this controversy, we compare different power purchase scenarios, considering major uncertainty factors such as electricity prices and the availability of renewables in various European locations. We show that the permission for unrestricted electricity mix usage does not necessarily lead to an emission intensity increase, partially debilitating concerns by the European Commission, and could notably decrease green hydrogen production cost. Furthermore, our results indicate that the transitional regulations adopted to support a green hydrogen production ramp-up can result in similar cost reductions and ensure high renewable electricity usage.

Integrating spin-dependent emission and dielectric switching in FeII catenated metal-organic frameworks

Mechanically interlocked molecules (MIMs) including famous catenanes show switchable physical properties and attract continuous research interest due to their potential application in molecular devices. The advantages of using spin crossover (SCO) materials here are enormous, allowing for control through diverse stimuli and highly specific functions, and enabling the transfer of the internal dynamics of MIMs from solution to solid state, leading to macroscopic applications. Herein, we report the efficient self-assembly of catenated metal-organic frameworks (termed catena-MOFs) induced by stacking interactions, through the combination of rationally selected flexible and conjugated naphthalene diimide-based bis-pyridyl ligand (BPND), [MI(CN)2]− (M = Ag or Au) and Fe2+ in a one-step strategy. The obtained bimetallic Hofmann-type SCO-MOFs [FeII(BPND){Ag(CN)2}2]·3CHCl3 (1Ag) and [FeII(BPND{Au(CN)2}2]·2CHCl3·2H2O (1Au) possess a unique three-dimensional (3D) catena-MOF constructed from the polycatenation of two-dimensional (2D) layers with hxl topology. Both complexes undergo thermal- and light-induced SCO. Significantly, abnormal increases in the maximum emission intensity and dielectric constant can be detected simultaneously with the switching of spin states. This research opens up SCO-actuated bistable MIMs that afford dual functionality of coupled fluorescence emission and dielectricity.